Literature DB >> 20111794

Open-cage fullerenes: towards the construction of nanosized molecular containers.

Georgios C Vougioukalakis1, Manolis M Roubelakis, Michael Orfanopoulos.   

Abstract

Open-cage fullerene derivatives have excited organic chemists' creativity over the past decade. These adducts, generated via consecutive cleavage of sigma- and pi-carbon-carbon bonds on the fullerene cage, allow small atoms or molecules to pass through their opening and be placed inside the cavity. Restoration of the ruptured fullerene back to the pristine fullerene cage affords the corresponding endohedral complexes. This "molecular surgery" approach has been proposed as an alternative to the synthesis of endohedral fullerenes via the conventional physical methods of production, which restrict the availability of endohedral fullerenes to milligram quantities after laborious isolation procedures. In this critical review, we survey all published techniques for the creation of an orifice, as well as for the expansion of an existing one, on the fullerene framework. Successful encapsulation experiments employing cage-opened fullerene derivatives are also comprehensively discussed (160 references).

Entities:  

Year:  2009        PMID: 20111794     DOI: 10.1039/b913766a

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  11 in total

1.  Reversible Diels-Alder Addition to Fullerenes: A Study of Dimethylanthracene with H2@C60.

Authors:  Mahboob Subhani; Jinrong Zhou; Yuguang Sui; Huijing Zou; Michael Frunzi; James Cross; Martin Saunders; Cijun Shuai; Wenjie Liang; Hai Xu
Journal:  Nanomaterials (Basel)       Date:  2022-05-13       Impact factor: 5.719

2.  Synthesis of a distinct water dimer inside fullerene C70.

Authors:  Rui Zhang; Michihisa Murata; Tomoko Aharen; Atsushi Wakamiya; Takafumi Shimoaka; Takeshi Hasegawa; Yasujiro Murata
Journal:  Nat Chem       Date:  2016-03-07       Impact factor: 24.427

3.  Carbon arc production of heptagon-containing fullerene[68].

Authors:  Yuan-Zhi Tan; Rui-Ting Chen; Zhao-Jiang Liao; Jia Li; Feng Zhu; Xin Lu; Su-Yuan Xie; Jun Li; Rong-Bin Huang; Lan-Sun Zheng
Journal:  Nat Commun       Date:  2011-08-09       Impact factor: 14.919

4.  Synthesis and Properties of Open Fullerenes Encapsulating Ammonia and Methane.

Authors:  Sally Bloodworth; John Gräsvik; Shamim Alom; Karel Kouřil; Stuart J Elliott; Neil J Wells; Anthony J Horsewill; Salvatore Mamone; Mónica Jiménez-Ruiz; Stéphane Rols; Urmas Nagel; Toomas Rõõm; Malcolm H Levitt; Richard J Whitby
Journal:  Chemphyschem       Date:  2018-01-04       Impact factor: 3.102

5.  Vibronic Coupling in Spherically Encapsulated, Diatomic Molecules: Prediction of a Renner-Teller-like Effect for Endofullerenes.

Authors:  Andreas W Hauser; Johann V Pototschnig
Journal:  J Phys Chem A       Date:  2022-03-08       Impact factor: 2.944

6.  An orifice design: water insertion into C60.

Authors:  Yoshifumi Hashikawa; Kazuro Kizaki; Takashi Hirose; Yasujiro Murata
Journal:  RSC Adv       Date:  2020-11-06       Impact factor: 4.036

7.  Isolation of the simplest hydrated acid.

Authors:  Rui Zhang; Michihisa Murata; Atsushi Wakamiya; Takafumi Shimoaka; Takeshi Hasegawa; Yasujiro Murata
Journal:  Sci Adv       Date:  2017-04-21       Impact factor: 14.136

Review 8.  Nanoscale Hollow Spheres: Microemulsion-Based Synthesis, Structural Characterization and Container-Type Functionality.

Authors:  Henriette Gröger; Christian Kind; Peter Leidinger; Marcus Roming; Claus Feldmann
Journal:  Materials (Basel)       Date:  2010-08-12       Impact factor: 3.623

Review 9.  Synthesis of Doped/Hybrid Carbon Dots and Their Biomedical Application.

Authors:  Vijay Bhooshan Kumar; Ze'ev Porat; Aharon Gedanken
Journal:  Nanomaterials (Basel)       Date:  2022-03-08       Impact factor: 5.076

Review 10.  Direct Photocatalyzed Hydrogen Atom Transfer (HAT) for Aliphatic C-H Bonds Elaboration.

Authors:  Luca Capaldo; Davide Ravelli; Maurizio Fagnoni
Journal:  Chem Rev       Date:  2021-08-06       Impact factor: 60.622

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